| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90437-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-06497-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98267-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12073-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26172-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26542-50ul | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Alexa Fluor 488 | DDX0321A488-100 | |||
| Alexa Fluor 546 | DDX0321A546-100 | |||
| Alexa Fluor 647 | DDX0321A647-100 | |||
![Flow Cytometry: L-Selectin/CD62L Antibody (DREG56) [NBP1-42795] - Surface staining pattern of human peripheral blood stained using anti-human CD62L (DREG56) purified antibody (concentration in sample 1 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/L-Selectin-CD62L-Antibody-DREG56-Flow-Cytometry-NBP1-42795-img0015.jpg "Flow Cytometry: L-Selectin/CD62L Antibody (DREG56) [NBP1-42795] - Surface staining pattern of human peripheral blood stained using anti-human CD62L (DREG56) purified antibody (concentration in sample 1 ug/ml) GAM APC.")
![Flow Cytometry: L-Selectin/CD62L Antibody (DREG56) [NBP1-42795] - Separation of human CD62L positive lymphocytes (red-filled) from CD62L negative lymphocytes (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using anti-human CD62L (DREG56) purified antibody (concentration in sample 1 ug/ml) GAM APC.](http://images.novusbio.com/fullsize/L-Selectin-CD62L-Antibody-DREG56-Flow-Cytometry-NBP1-42795-img0014.jpg)
![Immunohistochemistry-Paraffin: SR-AI/MSR Antibody (004) [NBP2-90437] - Immunochemical staining of mouse SR-AI/MSR in mouse liver with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/SR-AI-MSR-Antibody-004-Immunohistochemistry-Paraffin-NBP2-90437-img0003.jpg "Immunohistochemistry-Paraffin: SR-AI/MSR Antibody (004) [NBP2-90437] - Immunochemical staining of mouse SR-AI/MSR in mouse liver with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).")
![Flow Cytometry: SR-AI/MSR Antibody (004) [NBP2-90437] - Flow cytometric analysis of Mouse SR-AI/MSR expression on Raw264.7 cells. Cells were stained with purified anti-Mouse SR-AI/MSR, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/SR-AI-MSR-Antibody-004-Flow-Cytometry-NBP2-90437-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: SR-AI/MSR Antibody (004) [NBP2-90437] - Confocal immunofluorescence analysis of Mouse SR-AI/MSR1 in RAW264.7 cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-90437 antibody (1:100) at 4C overnight. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG Secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to plasma membrane.](http://images.novusbio.com/fullsize/nbp2-90437_rabbit-monoclonal-sr-ai-msr-antibody-004-235202511444470.png)
![Western Blot: CYB5R3 Antibody [NBP3-06497] - Lane A: A431 Whole Cell LysateLane B: HepG2 Whole Cell LysateLane C: HeLa Whole Cell LysateLane D: U87MG Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:34 kDaObserved band size:34 kDa](http://images.novusbio.com/fullsize/CYB5R3-Antibody-Western-Blot-NBP3-06497-img0001.jpg "Western Blot: CYB5R3 Antibody [NBP3-06497] - Lane A: A431 Whole Cell LysateLane B: HepG2 Whole Cell LysateLane C: HeLa Whole Cell LysateLane D: U87MG Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:34 kDaObserved band size:34 kDa")
![Immunohistochemistry-Paraffin: CYB5R3 Antibody [NBP3-06497] - Staining of human CYB5R3 in human testis with rabbit polyclonal antibody at 1:10000 dilution.](http://images.novusbio.com/fullsize/CYB5R3-Antibody-Immunohistochemistry-Paraffin-NBP3-06497-img0002.jpg)
![Immunoprecipitation: CYB5R3 Antibody [NBP3-06497] - Lane A:0.5 mg A431 HepG2 HeLa U87MG Whole Cell Lysate4 uL anti-CYB5R3 rabbit polyclonal antibody and 60 ug of Immunomagnetic beads Protein A/G.Primary antibody:Anti-CYB5R3 rabbit polyclonal antibody,at 1:100 dilution Secondary antibody:Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilutionDeveloped using the ECL technique.Performed under reducing conditions.Predicted band size: 34 kDaObserved band size :34 kDa](http://images.novusbio.com/fullsize/CYB5R3-Antibody-Immunoprecipitation-NBP3-06497-img0003.jpg)
![Western Blot: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Western blot analysis of Myeloperoxidase/MPO on different lysates with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/5,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 84 kDa Observed band size: 84/55 kDa Exposure time: 24 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32624) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-2882024142265.jpg "Western Blot: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Western blot analysis of Myeloperoxidase/MPO on different lysates with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/5,000 dilution. Lane 1: HeLa cell lysate (negative) Lane 2: HL-60 cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 84 kDa Observed band size: 84/55 kDa Exposure time: 24 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32624) at 1/5,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32624) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-298202414161865.jpg)
![Immunocytochemistry/ Immunofluorescence: Myeloperoxidase/MPO Antibody (PD00-20) [NBP3-32624] - Immunocytochemistry analysis of Jurkat cells labeling Myeloperoxidase/MPO with Rabbit anti-Myeloperoxidase/MPO/MPO antibody (NBP3-32624) at 1/100 dilution. Cells were fixed in 80% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Myeloperoxidase/MPO antibody (NBP3-32624) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32624_rabbit-myeloperoxidase-mpo-mab-pd00-20-29202410234294.jpg)
![Immunohistochemistry: Adiponectin/Acrp30 Antibody (JE65-49) [NBP3-32003] - Immunohistochemical analysis of paraffin-embedded mouse large intestine tissue with Rabbit anti-Adiponectin/Acrp30 antibody (NBP3-32003) at 1/400 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32003) at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp3-32003_rabbit-adiponectin-acrp30-mab-je65-49-2982024149262.jpg "Immunohistochemistry: Adiponectin/Acrp30 Antibody (JE65-49) [NBP3-32003] - Immunohistochemical analysis of paraffin-embedded mouse large intestine tissue with Rabbit anti-Adiponectin/Acrp30 antibody (NBP3-32003) at 1/400 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32003) at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.")
![Immunocytochemistry/ Immunofluorescence: Adiponectin/Acrp30 Antibody (JE65-49) [NBP3-32003] - Immunocytochemistry analysis of NCI-H441 cells labeling Adiponectin/Acrp30 with Rabbit anti-Adiponectin/Acrp30 antibody (NBP3-32003) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-Adiponectin/Acrp30 antibody (NBP3-32003) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 647) were used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32003_rabbit-adiponectin-acrp30-mab-je65-49-29202410484876.jpg)
![Western Blot: Adiponectin/Acrp30 Antibody (JE65-49) [NBP3-32003] - Western blot analysis of Adiponectin/Acrp30 on mouse colon tissue lysates with Rabbit anti-Adiponectin/Acrp30 antibody (NBP3-32003) at 1/500 dilution. Lysates/proteins at 20 ug/Lane. Predicted band size: 27 kDa Observed band size: 34 kDa Exposure time: 2 minutes; 12% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32003) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32003_rabbit-adiponectin-acrp30-mab-je65-49-392024848505.jpg)
![Western Blot: Angiopoietin-like Protein 4/ANGPTL4 Antibody [NBP2-98267] - Lane A: Mouse liver tissue lysateLane B: Mouse skeletal muscle tissue lysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution.Developed using the Odyssey technique.Performed under reducing conditions.Predicted band size:45 kDaObserved band size:54 kDa](http://images.novusbio.com/fullsize/Angiopoietin-like-Protein-4-ANGPTL4-Antibody-Western-Blot-NBP2-98267-img0005.jpg "Western Blot: Angiopoietin-like Protein 4/ANGPTL4 Antibody [NBP2-98267] - Lane A: Mouse liver tissue lysateLane B: Mouse skeletal muscle tissue lysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution.Developed using the Odyssey technique.Performed under reducing conditions.Predicted band size:45 kDaObserved band size:54 kDa")
![Immunohistochemistry-Paraffin: Angiopoietin-like Protein 4/ANGPTL4 Antibody [NBP2-98267] - Immunochemical staining of mouse Angiopoietin-like Protein 4/ANGPTL4 in mouse skeletal muscle with rabbit polyclonal antibody (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/Angiopoietin-like-Protein-4-ANGPTL4-Antibody-Immunohistochemistry-Paraffin-NBP2-98267-img0004.jpg)
![Immunohistochemistry-Paraffin: Angiopoietin-like Protein 4/ANGPTL4 Antibody [NBP2-98267] - Immunochemical staining of mouse Angiopoietin-like Protein 4/ANGPTL4 in mouse heart with rabbit polyclonal antibody (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/Angiopoietin-like-Protein-4-ANGPTL4-Antibody-Immunohistochemistry-Paraffin-NBP2-98267-img0002.jpg)
![Immunohistochemistry-Paraffin: Angiopoietin-like Protein 4/ANGPTL4 Antibody [NBP2-98267] - Immunochemical staining of mouse Angiopoietin-like Protein 4/ANGPTL4 in mouse pancreas with rabbit polyclonal antibody (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/Angiopoietin-like-Protein-4-ANGPTL4-Antibody-Immunohistochemistry-Paraffin-NBP2-98267-img0003.jpg)
![Western Blot: SR-BI Antibody (185-1G2 (B467)) - Chimeric [NBP3-12073] - Human peripheral blood monocyte cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 185-1G2 (B467) (NBP3-12073) at 0.03 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.](http://images.novusbio.com/fullsize/SR-BI-Antibody-185-1G2-B467-Chimeric-Western-Blot-NBP3-12073-img0001.jpg "Western Blot: SR-BI Antibody (185-1G2 (B467)) - Chimeric [NBP3-12073] - Human peripheral blood monocyte cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 185-1G2 (B467) (NBP3-12073) at 0.03 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.")
![Immunocytochemistry /Immunofluorescence: SR-BI Antibody (185-1G2 (B467)) - Chimeric - Azide and BSA Free [NBP3-12073] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on Shi-fix(TM) coverslips stained with NBP3-12073 at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-12073, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-12073_rabbit-monoclonal-sr-bi-antibody-185-1g2-b467-chimeric-74202522141242.png)
![Western Blot: GSK-3 beta Antibody (M131) [NBP3-23366] - Western blot analysis of a human recombinant GSK-3 beta N-terminal fragment (lanes 1 & 2) and endogenous GSK-3 beta expressed in mouse brain (lanes 3 & 4). The blot was probed with mouse monoclonal anti-GSK-3 beta at 1:500 (lanes 1 & 3) and 1:2000 (lanes 2 & 4).](http://images.novusbio.com/fullsize/nbp3-23366_mouse-gsk-3-beta-mab-m131-1992023199282.jpg "Western Blot: GSK-3 beta Antibody (M131) [NBP3-23366] - Western blot analysis of a human recombinant GSK-3 beta N-terminal fragment (lanes 1 & 2) and endogenous GSK-3 beta expressed in mouse brain (lanes 3 & 4). The blot was probed with mouse monoclonal anti-GSK-3 beta at 1:500 (lanes 1 & 3) and 1:2000 (lanes 2 & 4).")
![Immunocytochemistry/Immunofluorescence: GSK-3 beta Antibody (M131) [NBP3-23366] - Immunocytochemical labeling of GSK-3 beta in aldehyde-fixed and NP-40 permeabilized human NCI-H1915 lung carcinoma cells. The cells were labeled with mouse monoclonal anti-GSK-3 beta (NBP3-23366) antibody. The antibody was detected using appropriate secondary antibody conjugated to DyLight(R) 594.](http://images.novusbio.com/fullsize/nbp3-23366_mouse-gsk-3-beta-mab-m131-19920231252364.jpg)
![Immunohistochemistry: LDLR Antibody (2B10) [NBP3-26172] - Image of LDLR Antibody (2B10) diluted at 1:100 and staining in paraffin-embedded human adrenal gland tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26172_rabbit-ldlr-mab-2b10-262202415475620.jpg "Immunohistochemistry: LDLR Antibody (2B10) [NBP3-26172] - Image of LDLR Antibody (2B10) diluted at 1:100 and staining in paraffin-embedded human adrenal gland tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: LDLR Antibody (2B10) [NBP3-26172] - Image of LDLR Antibody (2B10) diluted at 1:100 and staining in paraffin-embedded human adrenal gland tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26172_rabbit-ldlr-mab-2b10-27220248313719.jpg)
![Immunocytochemistry/Immunofluorescence: LDLR Antibody (2B10) [NBP3-26172] - Staining of Hela Cells with LDLR Antibody (2B10) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26172_rabbit-ldlr-mab-2b10-282202412493641.jpg)
![Flow Cytometry: LDLR Antibody (2B10) [NBP3-26172] - Overlay histogram showing Hela cells stained with LDLR Antibody (2B10) (red line) at 1:50. The cells were incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min at 4C. Control antibody (green line) was Rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26172_rabbit-ldlr-mab-2b10-282202414183657.jpg)
![Immunohistochemistry: GSK-3 beta Antibody (9G11) [NBP3-26542] - Image of GSK-3 beta Antibody (9G11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-262202414471519.jpg "Immunohistochemistry: GSK-3 beta Antibody (9G11) [NBP3-26542] - Image of GSK-3 beta Antibody (9G11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Western Blot: GSK-3 beta Antibody (9G11) [NBP3-26542] - Positive Western Blot detected in: Hela whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate, 293 whole cell lysate. All lanes: GSK3 beta Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 47, 49 kDa Observed band size: 47 kDa](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-28220241140910.jpg)
![Immunocytochemistry/Immunofluorescence: GSK-3 beta Antibody (9G11) [NBP3-26542] - Staining of Hela Cells with GSK-3 beta Antibody (9G11) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26542_rabbit-gsk-3-beta-mab-9g11-282202412475130.jpg)
![Flow Cytometry: CD39/ENTPD1 Antibody (AC2.5) [DDX0321P-100]](http://images.novusbio.com/fullsize/CD39-ENTPD1-Antibody-AC2-5-Flow-Cytometry-DDX0321P-100-img0001.jpg "Flow Cytometry: CD39/ENTPD1 Antibody (AC2.5) [DDX0321P-100]")